On the Cytology and Taxonomic Position of Nudispora biformis N. G., N. Sp. (Microspora, Thelohaniidae), a Microsporidian Parasite of the Dragon Fly Coenagrion hastulatum in Sweden

The microsporidium Nudispora biformis n. g., n. sp., a parasite of a larva of the damsel fly Coenagrion hastulatum in Sweden, is described based on light microscopic and ultrastructural characteristics. Merogonial stages and sporonts are diplokaryotic. Sporogony comprises meiotic and mitotic divisions, and finally eight monokaryotic sporoblasts are released from a lobed plasmodium. Sporophorous vesicles are not formed. The monokaryotic spores are oval, measuring 1.4–1.8 × 2.8–3.4 μm in living condition. The thick spore wall has a layered exospore, with a median double-layer. The polaroplast has two lamellar parts, with the closest packed lamellae anteriorly. The isofilar polar filament is arranged in 6 (to 7) coils in the posterior half of the spore. Laminar and tubular extracellular material of exospore construction is present in the proximity of sporogonial stages. In addition to normal spores teratological spores are produced. The microsporidium is compared to the microsporidia of the Odonata; its possible relations to the genus Pseudothelohania and to the Thelohania-like microsporidia are discussed. The new genus is provisionally included in the family Thelohaniidae.     

The Light and Electron Microscopic Cytology of Janacekia adipophila N. Sp. (Microspora, Tuzetiidae), a Microsporidian Parasite of Ptychoptera paludosa (Diptera, Ptychopteridae)

ABSTRACT. The microsporidium Janacekia adipophila n. sp., a parasite of Ptychoptera paludosa larvae in Sweden, is described based on light microscopic and ultrastructural characteristics. Merogonial stages and sporonts are diplokaryotic. Merozoites are formed by rosette-like division. Sporonts develop into sporogonial plasmodia with isolated nuclei. These plasmodia give rise to 8–16 sporoblasts by rosette-like budding. A sporophorous vesicle is initiated by the sporogonial plasmodium. Sporoblasts and spores are enclosed in individual sporophorous vesicles. Granular inclusions of the vesicles, visible using light microscopy, discriminate sporogonial stages from stages of the merogony. The monokaryotic, fresh spores are oval with blunt ends, measuring 4.2-6.3 × 9.1-11.2 μm. Macrospores are formed in small numbers. The spore wall has three subdivisions and the exospore is electron-dense. The polaroplast has two parts: closely arranged lamellae anteriorly, wider sac-like compartments posteriorly. The isofilar polar filament, 191–264 nm wide, has 12-13 coils, which are arranged in one layer in the posterior half of the spore. The electron-dense inclusions of the sporophorous vesicle are modified during sporogony, and vesicles with mature spores are traversed by 21–27 nm wide tubules, which connect the exospore with the envelope of the vesicle. The walls of the tubules, the envelope of the vesicles, and the surface layer of the exospore are all identical double-layered structures. The microsporidium is compared to microsporidia of Ptychopteridae and Tipulidae and to related microsporidia of the family Tuzetiidae.     

Wittmannia antarctica N. G., N. Sp. (Nosematidae), a New Hyperparasite in the Antarctic Dicyemid Mesozoan Kantharella antarctica

ABSTRACT. Collections of the dicyemid mesozoan Kantharella antarctica were made in the Weddell Sea during the Antarctic Expedition of the research vessel RV Polarstern in 1990 and 1991. A diplokaryotic microsporidian was found infecting all nematogens from all the samples taken in both years. The infected cells contained all developmental stages. Merogony initially was monokaryotic and spoorogony of diplokaryotic sporonts was by multiple fission. The stained ovoidal spores measured between 4.3-6 μm X 1.7-2.3 μm. The ultrastructural findings come from 11 specimens of Kantharella antarctica that were cut in serial sections. All developmental stages were noteworthy because of the myelinosomes situated adjacent to each diplokaryon. Similarly conspicuous were some organelles in the spore: a prominent, extraordinarily electron dense anterior portion of the polaroplast and the posterior vacuole. The isofilar polar filament with a diameter of about 115 nm showed 9-11 coils. The great number of empty spore cases together with an extruded polar filament are indicative of an autoinfection. Though these characteristics resemble in part those of the genus Nosema from the family Nosematidae, the species in Kantharella antarctica differs from the former by its unusual development, life cycle and unusual host. Thus, this new species has been placed in a new genus and the name Wittmannia antarctica proposed.     

Unikaryon polygraphi sp.n. (Protista, Microspora): a new pathogen of the four-eyed spruce bark beetle Polygraphus poligraphus (Col., Scolytidae)

The microsporidium Unikaryon polygraphi sp.n., a pathogen of Polygraphus poligraphus in Austria is described based on light microscopic and ultrastructural characteristics. All life stages have isolated nuclei. Sporogony ends with uninucleate single sporoblasts and spores. Mature oval spores measure 2.5–3.0 μm × 1.0–1.5 μm. The larger spores (3 × 1.5 μm) belong to the `early spore type' with a polar filament coiled in five turns and the smaller spores (2.5 × 1 μm) with polar filament coiled in 6/7 turns belong to the `environmental spore type'. Columnar cells of the midgut, longitudinal and circular muscles and the secretory part of Malpighian tubules of adult beetles are infected. Mature spores are excreted together with the faeces.     

Henneguya adherens N. Sp. (Myxozoa, Myxosporea), Parasite of the Amazonian Fish, Acestrorhynchus falcatus

ABSTRACT. A new species of myxosporean from the gill filaments of the freshwater teleost fish, Acestrorhynchus falcatus collected in the Amazon river is described from light and transmission electron microscope observations. The mature spores (total length 32.3 [30.7–35.1] μ) and all developmental stages were found in the same sporogonic plasmodium. The ellipsoidal spore body consists of 2 unequal shell valves adhering together along the suture lines. Each valve, tapering as a caudal projection, forms a long tail (length 20.5 [18.0–21.7] μm). The tail was surrounded by a homogeneous sheath on its length. The polar capsules measuring 3.1 × 1.2 μm contain 3–4 coils of the polar filament. All surfaces of the immature and mature spores were surrounded by a closely adherent homogenous structural sheath, mainly thicker around the tails. The taxonomic affinities of this parasite to other species are discussed.     

Napamichum cellatum N. Sp. (Microspora, Thelohaniidae), a New Parasite of Midge Larvae of the Genus Endochironomus (Diptera, Chironomidae) in Sweden

ABSTRACT The new microsporidium, Napamichum cellatum, a parasite of the adipose tissue of midge larva of the genus Endochironomus in Sweden, is described based on light microscopic and ultrastructural characteristics. Plurinucleate Plasmodia with nuclei arranged as diplokarya divide, probably by plasmotomy, producing a small number of diplokaryotic merozoites. The number of merogonial cycles is unknown. Each diplokaryotic sporont yields eight monokaryotic sporoblasts in a thin-walled, more or less fusiform sporophorous vesicle. A small number of multisporoblastic sporophorous vesicles were observed, in which a part of the sporoblasts were anomalous. The sporogony probably begins with a meiotic division. The mature spores are slightly pyriform. Fixed and stained spores measure 2.1-2.4 × 3.7-4.5 μm. The five-layered spore wall is of the Napamichum type. The polar filament is anisofilar with seven to eight coils (142-156 and 120 nm wide). The angle of tilt is 55-65°. The polaroplast has an anterior lamellar and a posterior tubular part. The granular, tubular and crystal-like inclusions of the episporontal space disappear more or less completely when the spores mature. The crystal-like inclusions are prominent in haematoxylin staining, but not visible with the Giemsa technique. The microsporidium is compared to other octosporoblastic microsporidia of midge larva and to the species of the genera Chapmanium and Napamichum.     

Description of Chytridiopsis Trichopterae N. Sp. (Microspora, Chytridiopsidae), A Microsporidian Parasite of the Caddis Fly Polycentropus Flavomaculatus (Trichoptera, Polycentropodidae), With Comments On Relationships Between the Families Chytridiopsidae and Metchnikovellidae

ABSTRACT. The microsporidium Chytridiopsis trichopterae n. sp., a parasite of the midgut epithelium of larvae of the caddis fly Polycentropus flavomaculatus found in southern Sweden, is described based on light microscopic and ultrastructural characteristics. All life cycle stages have isolated nuclei. Merogonial reproduction was not observed. the sporogony comprises two sequences: one with free spores in parasitophorous vacuoles, the other in spherical, 5.6-6.8 μm wide, sporophorous vesicles which lie in the cytoplasm. the free sporogony yields more than 20 spores per sporont. the vesicle-bound sporogony produces 8, 12 or 16 spores. the envelope of the sporophorous vesicle is about 82 nm thick and layered. the internal layer is the plasma membrane of the sporont; the surface layer is electron dense with regularly arranged translucent components. Both spore types are spherical. They have an ～ 35-nm thick spore wall, with a plasma membrane, an electron-lucent endospore, and an ～ 14-nm thick electron-dense exospore. the polar sac is cup-like and lacks a layered anchoring disc. the polar filament is arranged in two to three isofilar coils in the half of the spore opposite the nucleus. the coupling between the polar sac and the polar filament is characteristic. the surface of the polar filament is covered with regularly arranged membraneous chambers resembling a honeycomb. There is no polaroplast of traditional type. the cytoplasm lacks polyribosomes. the nucleus has a prominent, wide nucleolus. the two spore types have identical construction, but differ in dimensions and electron density. Free living spores are about 3.2 μm wide, the diameter of the polar filament proper is 102-187 nm, the chambers of the honeycomb are 70-85 nm high, and the polar sac is up to 425 nm wide. Living spores in the vesicle-bound sporogony are about 2.1 μm wide, the polar filament measures 69-102 nm, the chambers of the honeycomb are about 45 nm high, and these spores are more electron dense. Comparisons of cytology (especially the construction of the spore wall and the polar filament and associated structures) and life cycles reveal prominent differences among the Chytridiopsis-like microsporidia, and close relationships between the families Chytridiopsidae and Metchnikovellidae.     

On the Cytology of Toxoglugea chironomi (Debaisieux, 1931) Jírovec 1936 (Microspora, Thelohaniidae)

ABSTRACT. The light microscopic and ultrastructural characteristics of a microsporidium provisionally identified as Toxoglugea chironomi (Debaiseux, 1931) Jírovec, 1936, is described. It was isolated from oenocytes and adipose tissue of a midge larva of the genus Dicrotendipes . Merozoites are diplokaryotic. The sporogony produces, by fragmentation, eight monokaryotic spores in a sporophorous vesicle. Mature spores are horse-shoe shaped. The total length is about 5.8 μm, the width 0.8-0.9 μm, the external height of the curve 2.3-3.5 μm, and the external width of the curve 3.5-5.2 μm. The polaroplast has lamellar compartments of two types: narrow and closely packed anteriorly, and wider and more loosely arranged posteriorly. The isofilar polar filament is arranged in 8–10 coils in the posterior fourth of the spore. The external nuclear membrane is sometimes continuous with the endoplasmic reticulum. Lamellar and tubular material of exospore construction are present in the episporontal space from the beginning of sporogony. Teratological and normal spores sometimes occur together in the sporophorous vesicle. The identification of the species is discussed and the ultrastructure is compared to Toxoglugea variabilis , the only further species of the genus with known ultrastructural cytology.     

Fine structure of the developing spore of Nosema apis zander

Summary The mature spore possesses a thick spore coat and a particle-bearing spore membrane. The highly laminated polaroplast membranes are located at the anterior pole of the spore. Close to its base, the polar filament is surrounded by the polaroplast membrane. The polar filament runs spirally towards the posterior pole of the spore. A large portion of the polar filament is arranged in two layers. A similar arrangement was also observed in immature spores and in the sporoblast stage, although it was not so orderly arranged in the latter. The developing polaroplast membrane was observed in the immature spore, but not in the sporoblast. The sporoblast wall is much thinner than the spore coat, but has the same texture. Endoplasmic reticulum is the most prominent cytoplasmic organelle in the developing stages of Nosema apis. Porous nuclear envelopes are also observed in developing stages. The role of the endoplasmic reticulum in the formation of the polar filament, polaroplast and spore coat, and the function of the spore membrane, are discussed.     

Vavraia lutzomyiae n. sp. (Phylum Microspora) infecting the sandfly Lutzomyia longipalpis (Psychodidae, Phlebotominae), a vector of human visceral leishmaniasis

Vavraia lutzomyiae (Microsporida; Pleistophoridae) is a new species parasitic in the tropical phlebotomine sandfly, Lutzomyia longipalpis (Diptera, Psychodidae, Phlebotominae), a major vector of Leishmania chagasi in Latin America where human visceral leishmaniasis is endemic. Infected larvae and pupae were parasitized in the abdomen, and some adults were parasitized in Malpighian tubules and midgut. The sporogonial plasmodium divided by multiple divisions into up to 64 uninucleate sporoblasts. These stages were surrounded outside the plasmalemma by a thick, amorphous dense coat and transformed into a merontogenetic sporophorous vesicle within which the sporonts developed into sporoblasts. The mature microsporidian spores were broadly ellipsoidal and measured 6.1+/-0.43 x 3.1+/-0.15 microm. The spore wall consisted of a transparent endospore (approximately 100 nm) and a thin electron dense exospore (approximately 30 nm) with the outer limit slightly undulated. Spores contained a polar filament arranged peripherally in a single layer of eight to nine wide anterior coils (approximately 125 nm diameter), and three to four narrow posterior coils (approximately 70 nm diameter). Transverse sections revealed a concentric layer organization with the internal layer surrounded by numerous (up to 25) longitudinal microfibrils. The angle of tilt of the polar filament was about 65-68 degrees.     

Sphaerospora ovophila N. Sp. and Myxobolus algonquinensis N. Sp. (Myxozoa, Myxosporea), Ovarian Parasites of Fish from Algonquin Park, Ontario, Canada

ABSTRACT. Sphaerospora ovophila n. sp. and Myxobolus algonquinensis n. sp., found in the ovary of the pumpkinseed ( Lepomis gibbosus ) and the golden shiner ( Noremigonus crysoleucas ) respectively from Algonquin Park, Ontario, are described using light and electron microscopy. Ovoid cysts of S. ovophila measured up to 500 pm in length. Monosporic pseudoplasmodia were ovoid or ellipsoid in shape and measured up to 12.5 pm in length. Spores were 7.2–8.4 pm long × 6.0–7.0 pm wide (in sutural plane) × 7.4–8.2 pm thick (perpendicular to sutural plane), with two subspherical polar capsules of equal size measuring 2.7–3.2 × 2.6–3.1 pm and each of which contained a polar filament with 6–7 coils. The spore had a straight sutural ridge which protruded slightly at the anterior end and contained two uninucleate sporoplasms. The spore valve had ornate folds on the posterior end. Cysts of M. algonquinensis ranged from ovoid to elongated ellipsoid in shape and measured up to 800 pm in length. Mature spores measured 13.G15.7 pm long × 10.1–12.1 pm wide × 5.0–6.9 pm thick. with two pyriform polar capsules of equal size measuring 5.1–5.5 pm × 2.5–2.9 pm, each of which contained a polar filament with 4–6 coils. The spores of M. algonquinensis had smooth valves, a straight sutural ridge and a distinct small intercapsular appendix.     

Further Observations on the Fine Structure of the Spores of Glugea weissenbergi (Microsporida,Nosematidae)*

SYNOPSIS. A Glugea xenoma sectioned and viewed with the electron microscope contained many spores with everting polar filaments. Several details not seen in previous studies of this species were observed. A specialized area with the appareance of a lattice was commonly present near the anterior end of the polaroplast. The external portion of a partially everted polar filament appeared to have about twice the diameter of the part remaining within the spore. No membrane was seen limiting the external surface of the everted portion. The everting filament had pushed thru the polar cap and the adjacent thin area of the spore wall, making the polar cap into a ring. The ring connected the proximal end of the everting filament to the inner spore membrane, thereby anchoring the filament to the spore. The electron density of some of the membranous organelles of the spore was enhanced by the use of ruthenium red.     

Brachiola vesicularum, N. G., N. Sp., a New Microsporidium Associated with AIDS and Myositis

Brachiola vesicularum, n. g., n. sp., is a new microsporidium associated with AIDS and myositis. Biopsied muscle tissue, examined by light and electron microscopy, revealed the presence of organisms developing in direct contact with muscle cell cytoplasm and fibers. No other tissue types were infected. All parasite stages contain diplokaryotic nuclei and all cell division is by binary fission. Sporogony is disporoblastic, producing 2.9 times 2 μm diplokaryotic spores containing 8-10 coils of the polar filament arranged in one to three rows, usually two. Additionally, this microsporidium produces electron-dense extracellular secretions and vesiculotubular appendages similar to Nosema algerae. However, the production of protoplasmic extensions which may branch and terminate in extensive vesiculotubular structures is unique to this parasite. Additionally, unlike Nosema algerae , its development occurred at warm blooded host temperature (37-38° C) and unlike Nosema connori , which disseminates to all tissue types, B. vesicularum infected only muscle cells. Thus, a new genus and species is proposed. Because of the similarities with the genus Nosema , this new genus is placed in the family Nosematidae. Successful clearing of this infection (both clinically and histologically) resulted from treatment with albendazole and itraconozole.     

Occurrence of a new microsporidan: Enterocytozoon bieneusi n.g., n. sp., in the enterocytes of a human patient with AIDS

A new microsporidium is reported infesting the enterocytes of a Haitian patients with AIDS. The stages observed were diplokaryotic cells, sporogonial plasmodia, unikaryotic sporoblasts, and spores. Neither a sporophorous vesicle (pansporoblastic membrane) nor parasitophorous vacuole were differentiated around the developmental stages, which were in direct contact with the host cell cytoplasm. The polar tube (5-6 coils) was differentiated before fission of the sporogonial plasmodium. The mature spores measured 1.5 micron X 0.5 micron. The spore wall was very thin as the endospore was absent or poorly differentiated. The organism is named Enterocytozoon bieneusi n. g., n. sp. and is assigned to the suborder Apansporoblastina.     

Occurrence of a New Microsporidan: Enterocytozoon bieneusi n. g., n. sp., in the Enterocytes of a Human Patient with AIDS1

A new microsporidium is reported infesting the enterocytes of a Haitian patient with AIDS. The stages observed were diplokaryotic cells, sporogonial plasmodia, unikaryotic sporoblasts, and spores. Neither a sporophorous vesicle (pansporoblastic membrane) nor parasitophorous vacuole were differentiated around the developmental stages, which were in direct contact with the host cell cytoplasm. The polar tube (5-6 coils) was differentiated before fission of the sporogonial plasmodium. The mature spores measured 1.5 m?m × 0.5 m?. The spore wall was very thin as the endospore was absent or poorly differentiated. The organism is named Enterocytozoon bieneusi n. g., n. sp. and is assigned to the suborder Apansporoblastina.     

Ultrastructural Study of Endoreticulatus durforti N. Sp., a New Microsporidian Parasite of the Intestinal Epithelium of Artemia (Crustacea, Anostraca)

ABSTRACT. A new microsporidian parasite of the Artemia intestinal epithelium has been studied. The microsporidium developed within a membranous parasitophorous vesicle from the host rough endoplasmic reticulum consisting of two membranes, with the proximal one usually lacking ribosomes.
All developmental stages had isolated nuclei. Unikaryotic meronts developed into merogonial plasmodia. Merogonial division occurred by binary fission and rosette-shaped fragmentation. In young sporonts, an electron-lucent space, corresponding to the developing endospore, was immediately observed between both the plasmalemma and the exospore primordium. Sporogonial division occurred also by rosette-shaped fragmentation, resulting in at least eight sporoblasts that developed directly into spores. Fresh spores were 1.7 × 0.9 μm in size and oval-shaped. The 8–11 coil isofilar polar filament was arranged in two rows. The polaroplast was bipartite. The nature of the parasitophorous envelope, host-parasite interaction, developmental cycle and taxonomy are discussed.     

Heterovesicula cowani N. G., N. Sp. (Heterovesiculidae N. Fam.), a Microsporidian Parasite of Mormon Crickets, Anabrus simplex Haldeman, 1852 (Orthoptera: Tettigoniidae)

ABSTRACT. Heterovesicula cowani , n. g., n. sp., is a dimorphic microsporidium described from the adipose tissue of the Mormon cricket, Anabrus simplex Haldeman. Proliferation of the microsporidium is by karyokinesis of uninucleate and binucleate cells to form binucleate and tetranucleate cells, respectively. These cells will undergo binary fission (merogony). Ultimately, the meronts undergo karyokinesis without subsequent cytokinesis producing spherical multinucleate plasmodia that are transitional to 2 types of sporogony. Transitional to disporoblastic sporogony, a fragile interfacial envelope delaminates from the plasmodium with morphogenesis to a monfiliform plasmodium consisting of fusiform binucleate diplokaryotic sporonts. These undergo karyokinesis to form tetranucleate diplokaryotic sporonts that undergo cytokinesis during disintegration of the plasmodium into isolated binucleate sporonts. Transitional to octosporoblastic sporogony, multinucleate plasmodia disintegrate into short monofiliform plasmodia of diplokaryotic sporonts which then segregate while undergoing gradual nuclear dissociation (haplosis by nuclear dissociation). These undergo two sequences of karyokinesis and subsequent multiple fission to form eight uninucleate (haploid) sporoblasts in a fusiform arrangement within a persistent envelope. Binucleate spores are ovocylindrical, about 5.4 × 1.7 μm (fresh), with an isofilar polar filament singly coiled about 11 turns. Uninucleate spores are ovoid to slightly pyriform, 4.0 × 1.7 μm (fresh), with an isofilar filament singly coiled about 9 turns. A new family, Heterovesculidae, is proposed for the new genus.     

New species of Parathelohania (Microsporidia) in larva of the Anopheles aquasalis (Diptera: Culicidae) in Venezuela

The symptoms of Anopheles aquasalis larvae naturally infected by a microsporidium, and the ultrastructure of the infecting spores is described. The larvae were maintained under laboratory conditions in salt concentrations of 10 g/l and 20 g/l of water. Daily recordings of the mortality of the larvae were made and the dates of change of instar were noted. Infected larvae were processed for transmission electronic microscopy using conventional methods at pH 7.2 and 260 mOsm/l. The infection by the microsporidia was positively correlated with an increase in the mean duration of the fourth instar of 2.88 to 6.33 days in 10 g/l of salt and of 2.47 to 6.14 days in 20 g/l of salt. Larval mortality also increased by approximately 50% during this instar in both salt concentrations. Development time and survival were not affected during the other immature stages. The mature spores found in the intestines of infected larvae were barrel shaped and measured approximately 2.6 x 2.4 mm. The exospore has a collar shaped prolongation at the posterior end of the spore. The spores are uninuclear with a posterior vacuole. The polar filament is anisofilar with nine rings, five with a diameter of 58 nm each and four with a diameter of 23 nm each. The polarplast is lamellate, and more tightly packed in the apical region. The reduction of the survival of A. aquasalis larvae infected with the microsporidia, and the increase in the development time suggest that this parasite might have a potential as a biological control of this pest. The microsporidium described here has similar characteristics to that of the genus Parathelohania. I suggest that the microsporidium found in A. aquasalis represents a new species and I propose the name Parathelohania aquasalensis. This is the first report of a microsporidium from a dipteran in Venezuela.     

Ultrastructure and molecular characterization of a microsporidium, Tubulinosema hippodamiae, from the convergent lady beetle, Hippodamia convergens Guérin-Méneville

Hippodamia convergens, the convergent lady beetle, is available for aphid control in home gardens and in commercial food production systems throughout the United States and Canada. Beetles received from commercial insectaries for biological control are occasionally infected with a microsporidium. The objective of this study was to describe the pathogen by means of ultrastructure, molecular characterization and tissue pathology. All stages of the microsporidium were in direct contact with the host cell cytoplasm. Early developmental stages were proximal to mature spores and both were observed throughout the tissue sections that were examined. Merogony resulted from binary fission. Early-stage sporoblasts were surrounded by a highly convoluted plasma membrane and contained an electron-dense cytoplasm and diplokaryon. Ovoid to elongated late-stage sporoblasts were surrounded by a relatively complete spore wall. The polar filament, polaroplast, and anchoring disk were readily observed within the cell cytoplasm. Mature spores were typical of terrestrial microsporidia, with a thickened endospore surrounded by a thin exospore. Spores contained well-defined internal structures, including a diplokaryon, lamellar polaroplast and a slightly anisofilar polar filament with 10-14 coils arranged in a single or double row. A prominent indentation was evident at the apical end of the spore wall proximal to the anchoring disk. Aberrant spores were also observed. These had a fully developed endospore and exospore but lacked any discernable internal spore structures, and were, instead, filled with lamellar or vesicular structures. Typical and aberrant spores measured 3.58 ± 0.2 × 2.06 ± 0.2 μm (n = 10) and 3.38 ± 0.8 × 2.13 ± 0.2 μm (n = 10), respectively. Spores were observed in longitudinal muscle surrounding the midgut and within the fat body, Malpighian tubules, pyloric valve epithelium, ventral nerve cord ganglia, muscles and ovaries. The hindgut epithelium was often infected but the connective tissues were rarely invaded. The life cycle and pathology of the microsporidium bears some resemblance to Nosema hippodamiae, the only microsporidium reported from H. convergens by Lipa and Steinhaus in 1959. Molecular characterization of the pathogen genomic DNA revealed that it is 99% similar to Tubulinosema acridophagus and T. ratisbonensis, two pathogens that infect Drosophila melanogaster and 98% similar to T. kingi from D. willistoni. Based on similarities in pathogen ultrastructure and the molecular information gained during this study, we propose that the microsporidium in H. convergens be given the name Tubulinosema hippodamiae.     

Ultrastructural studies of Henneguya rhamdia n. sp. (Myxozoa) a parasite from the Amazon teleost fish, Rhamdia quelen (Pimelodidae)

Henneguya rhamdia n. sp. is described in the gill filaments of the teleost fish Rhamdia quelen, collected from the Peixe Boi River, State of Pará, Brazil. This myxosporean produced spherical to ellipsoidal plasmodia, up to 300 microm in diameter, which contained developmental stages, including spores. Several dense bodies up to 2 microm in diameter were observed among the spores. The spore body was ellipsoidal (13.1 microm in length, 5.2 microm in width, and 2.5 microm in thickness) and each of the two valves presented a tapering tail (36.9 microm in length). These valves surrounded the binucleated sporoplasm cell and two equal ellipsoidal polar capsules (4.7 x 1.1 microm), which contained 10-11 (rarely 12) polar filament coils. The sporoplasm contained sporoplasmosomes with a laterally eccentric dense structure with a half-crescent section. Based on the data obtained by electron microscopy and on the host specificity, the spores differed from previously described Henneguya species, mainly in their shape and size, number and arrangement of the polar filament coils, and sporoplasmosome morphology.